Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?

BACKGROUND: Osteochondroma generally occurs as a single lesion and it is not a heritable disease. When two or more osteochondroma are present, this condition represents a genetic disorder named hereditary multiple exostoses (HME). Growth hormone deficiency (GHD) has rarely been found in HME patients...

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Detalhes bibliográficos
Publicado no:Ital J Pediatr
Main Authors: Bozzola, Mauro, Gertosio, Chiara, Gnoli, Maria, Baronio, Federico, Pedrini, Elena, Meazza, Cristina, Sangiorgi, Luca
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2015
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4524199/
https://ncbi.nlm.nih.gov/pubmed/26239617
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13052-015-0162-2
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